The world of pharmaceuticals can be a confusing maze of regulations and bureaucracy and no one should have to find their way through it alone. Gyma’s Scientific and Regulatory Affairs team can guide you through each step of the process from R&D to analytical development to pre- and post-approval regulatory submissions.

A combination of expertise, care and attention to detail, this team is committed to seeing you through to a successful outcome. Fully versed in the latest technical, FDA and US DEA regulations information, they provide our clients with great insights into:

  • Drug Master File Reviews

  • Pharmaceutical Imports

  • Facility Inspections

  • Establishment Registrations

  • Drug Listings

Quality Support

We are proud that many of our clients have been with us for decades and much of that has to do with our integrity, expertise and follow-through. Our facilities are staffed with professionals who deliver our clients exactly what they are expecting. In fact, we conduct our own patent search for each product we carry. Our attention to quality can be seen in our personalized service, access to cost-effective drugs, and product deliveries that are accurate, complete and on time. That’s why we are the chosen Finished Dose Manufacturer for the American market and still growing.